Detection and Quantification of Plasmodium DNA in Dried Blood Spots Using a Commercial Real-Time PCR Assay and Filter Card System
Thomas Hanscheid1,2, Vera Codices2, Adrian J.F. Luty3, Ayola A. Adegnika1,4,5, Peter G. Kremsner1,5 and Martin P. Grobusch1,6
1Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon. 2Institute of Molecular Medicine and Institute of Microbiology, Lisbon Medical College, Lisbon, Portugal. 3Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. 4Department of Parasitol- ogy, Leiden University Medical Centre, Leiden, The Netherlands. 5Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany. 6Infectious Diseases Unit, Division of Clinical Microbiology and Infectious Diseases, National Health Laboratory Service and School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Abstract
Blood collected on FTA® filter cards was analysed qualitatively and quantitatively with real-time PCR and the results compared with expert microscopy performed on-site in Gabon. There was 100% concordance for fresh blood samples. However, correlation of quantitative PCR-results was rather weak (0.52) and reproducibility showed coefficients of variation ranging from 10%–90%.
Readers of this also read:
- Human Parasitic Diseases - communicating new knowledge equitably and logically
- Detection and Quantification of Plasmodium DNA in Dried Blood Spots Using a Commercial Real-Time PCR Assay and Filter Card System
- Adenomatoid Tumor of Testis
- Human Parasitic Diseases - communicating new knowledge equitably and logically
- Detection of Oxacillin Resistance in Staphylococcus aureus Isolated from the Neonatal and Pediatric Units of a Brazilian Teaching Hospital